HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113602Generated: October 28, 2026
Triethylamine → tert-butyl (3S)-3-aminopiperidine-1-carboxylate
https://huagongshe.com/reaction/2113602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (R)-1-Boc-3-hydroxypiperidine | HCID 1514398 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl (3S)-3-aminopiperidine-1-carboxylate | HCID 1501975 | — |
Reaction Steps
Methanesulfonyl chloride (9.56 mL, 124 mmol) was added dropwise over 10 minutes to a stirred solution of 1,1-dimethylethyl (3R)-3-hydroxypiperidine-1-carboxylate (20.7 g, 103 mmol) and triethylamine (21.5 mL, 154 mmol) in dichloromethane (300 mL) at 0° C. After stirring for 3 hour at 0° C., the reaction was quenched by addition of water. The organic phase was washed with brine, dried (MgSO4), filtered and evaporated in vacuo to give an oil. This was purified by flash chromatography on silica, eluting with ethyl acetate/cyclohexane (20:80 to 50:50), to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432280B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-7858c37462804c8fa89cbaf7bc52e010 |
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| Source note | uspto-grants-2008_10 |
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